Canonical Allele Identifier: CA433629539

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064186G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026753G>C , CM000665.2:g.49026753G>C	GRCh38
NC_000003.11:g.49064186G>C , CM000665.1:g.49064186G>C	GRCh37
NC_000003.10:g.49039190G>C	NCBI36
NG_012091.1:g.7690C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2793C>G	ENSP00000515567.1:p.Gly931=
ENST00000703937.1:c.*1854C>G	ENSP00000515568.1:n.*1854C>G
ENST00000326739.9:c.753C>G MANE Select	ENSP00000321584.4:p.Gly251=
ENST00000429182.6:c.753C>G	ENSP00000393525.2:p.Gly251=
ENST00000442157.2:c.678C>G	ENSP00000403502.2:p.Gly226=
ENST00000462980.2:n.1268C>G
ENST00000472328.2:n.819C>G
ENST00000491610.2:n.713C>G
ENST00000676607.1:n.1049C>G
ENST00000676627.1:n.1483C>G
ENST00000676708.1:n.2033C>G
ENST00000676864.1:n.1902C>G
ENST00000677010.1:c.789C>G	ENSP00000503089.1:p.Gly263=
ENST00000677108.1:n.2659C>G
ENST00000677168.1:n.1225C>G
ENST00000677185.1:n.1316C>G
ENST00000677205.1:n.1537C>G
ENST00000677344.1:n.2027C>G
ENST00000677480.1:c.*430C>G	ENSP00000504378.1:n.*430C>G
ENST00000677519.1:n.1463C>G
ENST00000677593.1:n.1309C>G
ENST00000677740.1:n.2258C>G
ENST00000677991.1:n.1926C>G
ENST00000678001.1:n.1246C>G
ENST00000678085.1:n.1309C>G
ENST00000678177.1:n.2602C>G
ENST00000678603.1:n.1831C>G
ENST00000678724.1:c.678C>G	ENSP00000503874.1:p.Gly226=
ENST00000678920.1:n.911C>G
ENST00000679019.1:n.1523C>G
ENST00000679117.1:c.*568C>G	ENSP00000503240.1:n.*568C>G
ENST00000679339.1:n.1594C>G
ENST00000326739.8:c.753C>G	ENSP00000321584.4:p.Gly251=
ENST00000429182.5:c.547C>G
ENST00000442157.1:c.678C>G	ENSP00000403502.1:p.Gly226=
ENST00000462980.1:n.655C>G
ENST00000491610.1:n.713C>G
NM_000884.2:c.753C>G	NP_000875.2:p.Gly251=
XM_006713128.2:c.963C>G	XP_006713191.1:p.Gly321=
XM_006713128.3:c.963C>G	XP_006713191.1:p.Gly321=
XM_017006349.1:c.888C>G	XP_016861838.1:p.Gly296=
XM_017006350.1:c.888C>G	XP_016861839.1:p.Gly296=
NM_000884.3:c.753C>G MANE Select	NP_000875.2:p.Gly251=